A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17142098



Internal ID21496646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139950797..139950892hg38UCSC Ensembl
chr7:139650596..139650691hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5576326
Supporting Variants
SamplesNA19238
Known GenesTBXAS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17142098
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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